Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2286503
rs2286503
3 7 22816987 intron variant C/T snv 0.48 0.800 1.000 1 2013 2013
dbSNP: rs71520386
rs71520386
1 7 22813902 intron variant C/T snv 0.13 0.700 1.000 1 2016 2016